Product NDC: | 10096-0206 |
Proprietary Name: | Solutions |
Non Proprietary Name: | OCTINOXATE, OXYBENZONE, OCTISALATE, AVOBENZONE |
Active Ingredient(s): | 20; 75; 30; 30 mg/mL; mg/mL; mg/mL; mg/mL & nbsp; OCTINOXATE, OXYBENZONE, OCTISALATE, AVOBENZONE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 10096-0206 |
Labeler Name: | Avon Products, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20100607 |
Package NDC: | 10096-0206-1 |
Package Description: | 100 mL in 1 BOTTLE, PUMP (10096-0206-1) |
NDC Code | 10096-0206-1 |
Proprietary Name | Solutions |
Package Description | 100 mL in 1 BOTTLE, PUMP (10096-0206-1) |
Product NDC | 10096-0206 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | OCTINOXATE, OXYBENZONE, OCTISALATE, AVOBENZONE |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 20100607 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Avon Products, Inc. |
Substance Name | AVOBENZONE; OCTINOXATE; OCTISALATE; OXYBENZONE |
Strength Number | 20; 75; 30; 30 |
Strength Unit | mg/mL; mg/mL; mg/mL; mg/mL |
Pharmaceutical Classes |